Canonical Allele Identifier: CA2275552748

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524669T= , CM000679.2:g.75524669T=	GRCh38
NC_000017.10:g.73520750T= , CM000679.1:g.73520750T=	GRCh37
NC_000017.9:g.71032345T=	NCBI36
NG_013041.1:g.13142T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*257T= MANE Select	ENSP00000327487.6:n.*257T=
ENST00000434205.8:c.*257T=	ENSP00000406559.4:n.*257T=
ENST00000545228.3:c.*337T=	ENSP00000438169.3:n.*337T=
ENST00000577197.2:n.1036T=
ENST00000579449.2:n.2578T=
ENST00000580013.6:n.2982T=
ENST00000679370.1:n.3360T=
ENST00000679429.1:c.*1296T=	ENSP00000505403.1:n.*1296T=
ENST00000679443.1:n.1907T=
ENST00000679782.1:c.*537T=	ENSP00000505995.1:n.*537T=
ENST00000679919.1:n.2109T=
ENST00000679928.1:c.*2390T=	ENSP00000506071.1:n.*2390T=
ENST00000680999.1:c.*257T=	ENSP00000504984.1:n.*257T=
ENST00000681282.1:c.*2025T=	ENSP00000506339.1:n.*2025T=
ENST00000333213.10:c.*257T=	ENSP00000327487.6:n.*257T=
ENST00000545228.2:c.1115T=
ENST00000577197.1:n.586T=
NM_207346.2:c.*257T=	NP_997229.2:n.*257T=
XM_005257229.2:c.*337T=	XP_005257286.1:n.*337T=
XM_006721821.2:c.*337T=	XP_006721884.1:n.*337T=
XM_011524616.1:c.*337T=	XP_011522918.1:n.*337T=
XM_011524618.1:c.*257T=	XP_011522920.1:n.*257T=
XR_243646.2:n.2070T=
XM_005257229.4:c.*337T=	XP_005257286.1:n.*337T=
XR_243646.4:n.2076T=
NM_207346.3:c.*257T= MANE Select	NP_997229.2:n.*257T=